EP2876173B9 - Manufacturing method of grain-oriented electrical steel sheet - Google Patents

Manufacturing method of grain-oriented electrical steel sheet Download PDF

Info

Publication number
EP2876173B9
EP2876173B9 EP12881480.3A EP12881480A EP2876173B9 EP 2876173 B9 EP2876173 B9 EP 2876173B9 EP 12881480 A EP12881480 A EP 12881480A EP 2876173 B9 EP2876173 B9 EP 2876173B9
Authority
EP
European Patent Office
Prior art keywords
steel sheet
annealing
hot
grain
rolled
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Active
Application number
EP12881480.3A
Other languages
German (de)
French (fr)
Other versions
EP2876173B1 (en
EP2876173A4 (en
EP2876173B8 (en
EP2876173A1 (en
Inventor
Kenichi Murakami
Yoshiyuki Ushigami
Fumiaki Takahashi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Steel Corp
Original Assignee
Nippon Steel and Sumitomo Metal Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=49948466&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP2876173(B9) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Nippon Steel and Sumitomo Metal Corp filed Critical Nippon Steel and Sumitomo Metal Corp
Priority to PL12881480T priority Critical patent/PL2876173T3/en
Publication of EP2876173A1 publication Critical patent/EP2876173A1/en
Publication of EP2876173A4 publication Critical patent/EP2876173A4/en
Publication of EP2876173B1 publication Critical patent/EP2876173B1/en
Application granted granted Critical
Publication of EP2876173B8 publication Critical patent/EP2876173B8/en
Publication of EP2876173B9 publication Critical patent/EP2876173B9/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F1/00Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
    • H01F1/01Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
    • H01F1/03Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
    • H01F1/12Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
    • H01F1/14Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys
    • H01F1/147Alloys characterised by their composition
    • H01F1/14766Fe-Si based alloys
    • H01F1/14775Fe-Si based alloys in the form of sheets
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/12Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties
    • C21D8/1216Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties the working step(s) being of interest
    • C21D8/1222Hot rolling
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/12Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties
    • C21D8/1216Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties the working step(s) being of interest
    • C21D8/1233Cold rolling
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/12Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties
    • C21D8/1244Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties the heat treatment(s) being of interest
    • C21D8/1255Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties the heat treatment(s) being of interest with diffusion of elements, e.g. decarburising, nitriding
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/12Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties
    • C21D8/1244Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties the heat treatment(s) being of interest
    • C21D8/1261Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties the heat treatment(s) being of interest following hot rolling
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/12Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties
    • C21D8/1244Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of articles with special electromagnetic properties the heat treatment(s) being of interest
    • C21D8/1272Final recrystallisation annealing
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D9/00Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
    • C21D9/46Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/001Ferrous alloys, e.g. steel alloys containing N
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/002Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/008Ferrous alloys, e.g. steel alloys containing tin
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/02Ferrous alloys, e.g. steel alloys containing silicon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/04Ferrous alloys, e.g. steel alloys containing manganese
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/06Ferrous alloys, e.g. steel alloys containing aluminium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/08Ferrous alloys, e.g. steel alloys containing nickel
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/12Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/16Ferrous alloys, e.g. steel alloys containing copper
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/20Ferrous alloys, e.g. steel alloys containing chromium with copper
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/22Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/24Ferrous alloys, e.g. steel alloys containing chromium with vanadium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/32Ferrous alloys, e.g. steel alloys containing chromium with boron
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/34Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of silicon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/60Ferrous alloys, e.g. steel alloys containing lead, selenium, tellurium, or antimony, or more than 0.04% by weight of sulfur
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C8/00Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals
    • C23C8/06Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases
    • C23C8/08Solid state diffusion of only non-metal elements into metallic material surfaces; Chemical surface treatment of metallic material by reaction of the surface with a reactive gas, leaving reaction products of surface material in the coating, e.g. conversion coatings, passivation of metals using gases only one element being applied
    • C23C8/24Nitriding
    • C23C8/26Nitriding of ferrous surfaces
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F1/00Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
    • H01F1/01Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
    • H01F1/03Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
    • H01F1/12Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
    • H01F1/14Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys
    • H01F1/16Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys in the form of sheets

Definitions

  • the present invention relates to a manufacturing method of a grain-oriented electrical steel sheet suitable for an iron core of a transformer (trans.) or the like.
  • a grain-oriented electrical steel sheet is a steel sheet which contains Si and in which crystal grains are highly integrated in a ⁇ 110 ⁇ 001> orientation (Goss orientation), and is used as a material of an iron core of a stationary induction device such as a transformer or the like.
  • the control of the orientation of crystal grains is conducted with catastrophic grain growth phenomenon called secondary recrystallization.
  • a slab is heated at a temperature of 1300°C or higher to solid-dissolve fine precipitates called inhibitors almost completely, and thereafter, is subjected to hot-rolling, cold-rolling, annealing, and so on, to cause fine precipitates to precipitate during the hot-rolling and the annealing.
  • a slab is heated at a temperature of lower than 1300°C, and thereafter, is subjected to hot-rolling, cold-rolling, decarburization annealing, a nitridation treatment, finish annealing, and so on, to cause AlN, (Al, Si)N, and so on to precipitate as an inhibitor during the nitridation treatment.
  • the former method is sometimes called high-temperature slab heating, and the latter method is sometimes called low-temperature slab heating or intermediate-temperature slab heating.
  • a core loss of a grain-oriented electrical steel sheet is classified into a hysteresis loss and an eddy current loss roughly.
  • the hysteresis loss is affected by a crystal orientation, a defect, a grain boundary, and so on.
  • the eddy current loss is affected by a thickness, an electrical resistance value, a 180-degree magnetic domain width, and so on.
  • EP 2 418 294 A1 discloses a method for producing an electromagnetic steel sheet wherein the surface temperature of the slab at the start of a continuous casting step and a slab reheating step is specified.
  • the present invention has an object to provide a manufacturing method of a grain-oriented electrical steel sheet allowing core loss to be improved effectively.
  • the present inventors found that by forming a large number of nuclei of grains in the Goss orientation before occurrence of secondary recrystallization, the number of grains in the Goss orientation after the secondary recrystallization can be increased, and by such an increase in the number of grains in the Goss orientation, core loss can be improved and further variations in core loss can also be decreased. Further, the present inventors also found that for the formation of nuclei, adjusting ranges of a Sn content and a P content in particular and conditions of hot-rolled sheet annealing is effective.
  • the present invention has been made based on the above-described knowledge, and the gist thereof is as follows.
  • composition of a slab, conditions of hot-rolled sheet annealing and so on are made appropriate, and thereby it is possible to improve core loss effectively without performing control of magnetic domains and so on.
  • Fig. 1 is a flowchart illustrating a manufacturing method of a grain-oriented electrical steel sheet according to an embodiment of the present invention.
  • present inventors found that the formation of a large number of nuclei of grains in the Goss orientation before occurrence of secondary recrystallization contributes to improvement of core loss and a decrease in variations in core loss, and that, for the formation of nuclei, adjusting ranges of a Sn content and a P content in particular and conditions of hot-rolled sheet annealing are effective.
  • Fig. 1 is a flowchart illustrating a manufacturing method of a grain-oriented electrical steel sheet according to the embodiment of the present invention.
  • % being the unit of the content of each component means mass%.
  • Step S1 casting of a molten steel for a grain-oriented electrical steel sheet having a predetermined composition is performed to make a slab.
  • the molten steel contains, for example, C: 0.025% to 0.075%, Si: 2.5% to 4.0%, Mn: 0.03% to 0.30%, acid-soluble Al: 0.010% to 0.060%, N: 0.0010% to 0.0130%, Sn: 0.02% to 0.20%, S: 0.0010% to 0.020%, and P: 0.010% to 0.080%.
  • the balance of the molten steel is Fe and inevitable impurities.
  • elements that form inhibitors in processes of manufacturing the grain-oriented electrical steel sheet and remain in the grain-oriented electrical steel sheet after purification by high-temperature annealing are also included in the inevitable impurities.
  • C is an element effective for controlling a structure obtained through primary recrystallization (primary recrystallization structure).
  • primary recrystallization structure primary recrystallization structure
  • the C content is set to 0.025% to 0.075%.
  • Si is an element quite effective for increasing electrical resistance of a grain-oriented electrical steel sheet to thereby decrease an eddy current loss constituting a part of a core loss.
  • the Si content is less than 2.5%, it is not possible to sufficiently suppress the eddy current loss.
  • the Si content exceeds 4.0%, cold working is difficult to be performed.
  • the Si content is set to 2.5% to 4.0%.
  • Mn increases specific resistance of a grain-oriented electrical steel sheet to decrease a core loss. Mn also exhibits a function of preventing occurrence of crack during hot rolling. When the Mn content is less than 0.03%, these effects cannot be obtained sufficiently. On the other hand, when the Mn content exceeds 0.30%, a magnetic flux density of a grain-oriented electrical steel sheet decreases. Thus, the Mn content is set to 0.03% to 0.30%.
  • Acid-soluble Al is an important element which forms AlN functioning as an inhibitor.
  • the content of acid-soluble Al is less than 0.010%, it is not possible to form a sufficient amount of AlN and thus inhibitor strength is insufficient.
  • the content of acid-soluble Al exceeds 0.060%, AlN coarsens, and thereby the inhibitor strength decreases.
  • the content of acid-soluble Al is set to 0.010% to 0.060%.
  • N is an important element that reacts with acid-soluble Al to thereby form AlN.
  • a nitridation treatment is performed after cold rolling, so that a large amount of N is not required to be contained in a steel for a grain-oriented electrical steel sheet, but when the N content is set to be less than 0.0010%, there is sometimes a case that a large load is required during manufacturing a steel.
  • the N content exceeds 0.0130%, a hole called blister is caused in a steel sheet during cold rolling.
  • the N content is set to 0.0010% to 0.0130%.
  • Sn contributes to the formation of nuclei of grains in the Goss orientation. Though details of the reason are unclear, it is inferably because by the addition of Sn, a slip system of Fe changes and a deformation style in deformation by rolling differs from the case of no Sn being added. Further, Sn improves the quality of an oxide layer formed during decarburization annealing, and also improves the quality of a glass film formed using the oxide layer during finish annealing. That is, Sn improves the magnetic property and suppresses variations in magnetic property, through the stabilization of formation of the oxide layer and the glass film. When the Sn content is less than 0.02%, these effects cannot be obtained sufficiently.
  • the Sn content exceeds 0.20%, there is sometimes a case that a surface of a steel sheet is difficult to be oxidized and thus the formation of a glass film is insufficient.
  • the Sn content is set to 0.02% to 0.20%.
  • MnS precipitates mainly affect the primary recrystallization to exhibit a function of suppressing locational variation in grain growth of the primary recrystallization due to the hot rolling.
  • S content is less than 0.0010%, this effect cannot be obtained sufficiently.
  • S content exceeds 0.020%, the magnetic property is likely to deteriorate.
  • the S content is set to 0.0010% to 0.020%.
  • P increases the specific resistance of a grain-oriented electrical steel sheet to decrease a core loss. Further, P contributes to the formation of nuclei of grains in the Goss orientation. Though details of this reason are unclear, similarly to Sn, it is inferably because by the addition of P, a slip system of Fe changes and a deformation style in deformation by rolling differs from the case of no P being added. When the P content is less than 0.010%, these effects cannot be obtained sufficiently. On the other hand, when the P content exceeds 0.080%, the cold rolling sometimes is difficult to be performed. Thus, the P content is set to 0.010% to 0.080%.
  • Cr improves the quality of an oxide layer formed during decarburization annealing, and also improves the quality of a glass film formed using the oxide layer during finish annealing. That is, Cr improves the magnetic property and suppresses variations in magnetic property, through the stabilization of formation of the oxide layer and the glass film.
  • the Cr content is preferably 0.20% or less. Further, in order to sufficiently obtain the above-described effects, the Cr content is preferably 0.002% or more.
  • the molten steel may also contain at least one selected from the group consisting of Sb: 0.002% to 0.20%, Ni: 0.002% to 0.20%, Cu: 0.002% to 0.40%, Se: 0.0005% to 0.02%, Bi: 0.0005% to 0.02%, Pb: 0.0005% to 0.02%, B: 0.0005% to 0.02%, V: 0.002% to 0.02%, Mo: 0.002% to 0.02%, and As: 0.0005% to 0.02%.
  • Sb 0.002% to 0.20%
  • Ni 0.002% to 0.20%
  • Cu 0.002% to 0.40%
  • Se 0.0005% to 0.02%
  • Bi 0.0005% to 0.02%
  • Pb 0.0005% to 0.02%
  • B 0.0005% to 0.02%
  • V 0.002% to 0.02%
  • Mo 0.002% to 0.02%
  • As: 0.0005% to 0.02% is an inhibitor strengthening element.
  • the slab is heated (Step S2).
  • the temperature of the heating is preferably set to 1250°C or lower from the viewpoint of energy saving.
  • a finishing temperature of the hot rolling is set to 950°C or lower.
  • the finishing temperature is higher than 950°C, a texture deteriorates in the subsequent processes and particularly the nuclei of grains in the Goss orientation, which are formed during decarburization annealing, are decreased.
  • the thickness of a hot-rolled steel sheet is not limited in particular, and is set to 1.8 mm to 3.5 mm, for example.
  • hot-rolled sheet annealing of the hot-rolled steel sheet is performed to thereby obtain an annealed steel sheet (Step S4).
  • the hot-rolled sheet annealing is performed at 800°C to 1200°C.
  • the temperature of the hot-rolled sheet annealing is lower than 800°C, recrystallization of the hot-rolled steel sheet (hot-rolled sheet) is insufficient and a texture after the cold rolling and the subsequent decarburization annealing deteriorates to thereby make it difficult to obtain a grain-oriented electrical steel sheet provided with a sufficient magnetic property.
  • a cooling rate from 750°C to 300°C is set to 10°C /second to 300°C /second.
  • the cooling rate in the temperature range is less than 10°C/second, a texture after the cold rolling and the subsequent decarburization annealing deteriorates to thereby make it difficult to obtain a grain-oriented electrical steel sheet provided with a sufficient magnetic property.
  • the cooling rate in the temperature range is greater than 300°C/second, a cooling facility is likely to be overloaded.
  • the cooling rate in the temperature range is preferably set to 20°C/second or more.
  • Step S5 the cold rolling of the annealed steel sheet is performed to thereby obtain a cold-rolled steel sheet.
  • the cold rolling is performed a plurality of times while intermediate annealing being performed therebetween.
  • the intermediate annealing is performed at a temperature of 750°C to 1200°C for 30 seconds to 10 minutes.
  • the number of times of the cold rolling and whether or not the intermediate annealing is performed are preferably determined according to the property and cost required for a grain-oriented electrical steel sheet to be obtained finally.
  • a reduction ratio in the cold rolling is set to 85% or more.
  • the reduction ratio is preferably set to 88% or more.
  • the reduction ratio is preferably set to 92% or less.
  • the reduction ratio is greater than 92%, similarly to the case of being less than 85%, grains deviated from the Goss orientation are generated in the subsequent secondary recrystallization.
  • the decarburization annealing is performed on the cold-rolled steel sheet in a moist atmosphere containing hydrogen and nitrogen, to thereby obtain a decarburization-annealed steel sheet (Step S6). Carbon in the steel sheet is removed by the decarburization annealing, and the primary recrystallization occurs.
  • the temperature of the decarburization annealing is not limited in particular, but when the temperature of the decarburization annealing, is lower than 800°C, grains obtained by the primary recrystallization (primary recrystallization grains) may be too small, and thus there is sometimes a case that the subsequent secondary recrystallization does not sufficiently occur. On the other hand, when the temperature of the decarburization annealing exceeds 950°C, the primary recrystallization grains may be too large, and thus there is sometimes a case that the subsequent secondary recrystallization does not sufficiently occur.
  • Step S8 an annealing separating agent containing MgO as its main component in a water slurry form is applied on the surface of the decarburization-annealed steel sheet, and the decarburization-annealed steel sheet is coiled. Then, batch-type finish annealing is performed on the coiled decarburization-annealed steel sheet to thereby obtain a coiled finish-annealed steel sheet (Step S8). The secondary recrystallization occurs through the finish annealing.
  • the nitridation treatment is performed between beginning of the decarburization annealing and occurrence of the secondary recrystallization in the finish annealing (Step S7). This is to form inhibitors of (Al, Si)N.
  • the above nitridation treatment may be performed during the decarburization annealing (Step S6), or may also be performed during the finish annealing (Step S8). In the case when it is performed during the decarburization annealing, the annealing may be performed in an atmosphere containing a gas having nitriding capability such as ammonia, for example.
  • the nitridation treatment may be performed at a heating zone or a soaking zone in a continuous annealing furnace, or the nitridation treatment may also be performed at a stage after the soaking zone.
  • a powder having nitriding capability such as MnN, for example, may be added to the annealing separating agent.
  • Step S9 a coating solution containing aluminum phosphate and colloidal silica as its main component is applied on the surface of the finish-annealed steel sheet and is baked to form an insulating film.
  • the grain-oriented electrical steel sheet can be manufactured as described above.
  • Example in this section means “reference example”.
  • Conditions and so on in these experiments are examples employed for confirming the applicability and effects disclosed in the present application, and the present invention is not limited to these examples.
  • hot-rolled steel sheets each having a thickness of 2.3 mm.
  • a finishing temperature of the hot rolling was set to 940°C.
  • annealing was performed on each of the hot-rolled sheets at 1100°C for 120 seconds, and thereafter the hot-rolled sheets were each soaked in a hot water bath to be cooled at a cooling rate of 35°C/s from 750°C to 300°C. Then, pickling was performed, and thereafter cold rolling was performed to thereby obtain cold-rolled steel sheets (cold-rolled sheets) each having a thickness of 0.23 mm. In the cold rolling, the rolling was performed by about 30 passes, and at two passes out of them, the hot-rolled sheets were each heated to 250°C to be subjected to the rolling immediately.
  • decarburization annealing was performed at 860°C for 100 seconds in a gas atmosphere containing water vapor, hydrogen, and nitrogen, and subsequently nitridation annealing was performed at 770°C for 20 seconds in a gas atmosphere containing hydrogen, nitrogen, and ammonia.
  • An increasing temperature rate in the decarburization annealing was set to 32°C/s.
  • an annealing separating agent containing MgO as its main component in a water slurry form was applied, and then finish annealing was performed at 1200°C for 20 hours.
  • Finish-annealed steel sheets were each water washed, and of each of the steel sheets, a single-sheet for magnetic measurement having a size of W60 ⁇ L300 mm was cut out. Then, application and baking of a coating solution containing aluminum phosphate and colloidal silica as its main component were performed. Thus, grain-oriented electrical steel sheets each having an insulating film attached thereto were manufactured.
  • the core loss W17/50 is the value of core loss obtained when the magnetic flux density of 1.7 T is applied at 50 Hz. Further, the difference between the maximum value and the minimum value is the index indicating variations in the core loss W17/50.
  • annealing temperature between 780°C and 1210°C for 110 seconds
  • a cooling method was changed and a cooling rate (CR) from 750°C to 300°C. was varied between 5°C/s and 295°C/s.
  • cooling method there can be cited air cooling, hot-water cooling using water at 100°C, hot-water cooling using water at 80°C, hot-water cooling using water at 70°C, hot-water cooling using water at 60°C, hot-water cooling using water at 40°C, water cooling (20°C) using water at 20°C, and ice salt-water cooling using ice salt water.
  • the annealing temperature (HA) and the cooling rate (CR) of each of the hot-rolled sheets are listed in Table 2. Thereafter, cold rolling was performed to thereby obtain cold-rolled steel sheets (cold-rolled sheets) each having a thickness of 0.23 mm.
  • the rolling was performed by about 30 passes, and at two passes out of them, the hot-rolled sheets were each heated to 250°C to be subjected to the rolling immediately.
  • decarburization annealing was performed at 850°C for 90 seconds in a gas atmosphere containing water vapor, hydrogen, and nitrogen, and subsequently nitridation annealing was performed at 750°C for 20 seconds in a gas atmosphere containing hydrogen, nitrogen, and ammonia.
  • An increasing temperature rate in the decarburization annealing was set to 33°C/s.
  • an annealing separating agent containing MgO as its main component in a water slurry form was applied, and then finish annealing was performed at 1200°C for 20 hours.
  • Finish-annealed steel sheets were each water washed, and of each of the steel sheets, a single-sheet for magnetic measurement having a size of W60 ⁇ L300 mm was cut out. Then, application and baking of a coating solution containing aluminum phosphate and colloidal silica as its main component were performed. Thus, grain-oriented electrical steel sheets each having an insulating film attached thereto were manufactured.
  • the finishing temperature (FT) was 930°C or lower
  • the annealing temperature (HA) was 1050°C to 1200°C
  • the cooling rate (CR) was 10°C/s to 50°C/s.
  • the annealing temperature (HA) was 1210°C, which was high, and the brittle deterioration was severe. Then, it was not possible to manufacture a grain-oriented electrical steel sheet because fracture was caused in the cold rolling.
  • annealing was performed at 1120°C for 10 seconds and further annealing was performed at 920°C for 100 seconds, and thereafter the hot-rolled sheets were each soaked in a hot water bath to be cooled at a cooling rate of 25°C/s from 750°C to 300°C. Then, pickling was performed, and thereafter cold rolling was performed to thereby obtain cold-rolled steel sheets (cold-rolled sheets) each having a thickness of 0.275 mm. In the cold rolling, the rolling was performed by 30 to 40 passes, and at one pass out of them, the hot-rolled sheets were each heated to 240°C to be subjected to the rolling immediately.
  • the heating to 240°C was omitted. Whether or not the heating was performed is listed in Table 3. Subsequently, on each of the cold-rolled sheets, decarburization annealing was performed at 850°C for 110 seconds in a gas atmosphere containing water vapor, hydrogen, and nitrogen, and subsequently nitridation annealing was performed at 750°C for 20 seconds in a gas atmosphere containing hydrogen, nitrogen, and ammonia. An increasing temperature rate in the decarburization annealing was set to 31°C/s. Then, an annealing separating agent containing MgO as its main component in a water slurry form was applied, and then finish annealing was performed at 1180°C for 20 hours.
  • Finish-annealed steel sheets were each water washed, and of each of the steel sheets, a single-sheet for magnetic measurement having a size of W60 ⁇ L300 mm was cut out. Then, application and baking of a coating solution containing aluminum phosphate and colloidal silica as its main component were performed. Thus, grain-oriented electrical steel sheets each having an insulating film attached thereto were manufactured.
  • the cold-rolling ratio in Table 3 is a value obtained from the thickness of the hot-rolled sheet (HG) and the thickness of the cold-rolled sheet (0.275 mm).
  • annealing was performed at 1080°C for 110 seconds, and thereafter the hot-rolled sheets were each soaked in a hot water bath to be cooled at a cooling rate of 32°C/s from 750°C to 300°C. Then, pickling was performed, and thereafter cold rolling was performed to thereby obtain cold-rolled steel sheets (cold-rolled sheets) each having a thickness of 0.230 mm. In the cold rolling, the rolling was performed by about 30 passes, and at one pass out of them, the hot-rolled sheets were each heated to 270°C to be subjected to the rolling immediately.
  • decarburization annealing was performed at 830°C for 80 seconds in a gas atmosphere containing water vapor, hydrogen, and nitrogen, and subsequently nitridation annealing was performed at 800°C for 30 seconds in a gas atmosphere containing hydrogen, nitrogen, and ammonia.
  • An increasing temperature rate (HR) in the decarburization annealing was varied between 15°C/s and 300°C/s.
  • the increasing temperature rate (HR) is listed in Table 4.
  • an annealing separating agent containing MgO as its main component in a water slurry form was applied, and then finish annealing was performed at 1190°C for 20 hours.
  • Finish-annealed steel sheets were each water washed, and of each of the steel sheets, a single-sheet for magnetic measurement having a size of W60 ⁇ L300 mm was cut out. Then, application and baking of a coating solution containing aluminum phosphate and colloidal silica as its main component were performed. Thus, grain-oriented electrical steel sheets each having an insulating film attached thereto were manufactured.
  • the present invention may be utilized in an industry of manufacturing electrical steel sheets and an industry of utilizing electrical steel sheets, for example.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Electromagnetism (AREA)
  • Manufacturing & Machinery (AREA)
  • Dispersion Chemistry (AREA)
  • Power Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Manufacturing Of Steel Electrode Plates (AREA)
  • Soft Magnetic Materials (AREA)

Description

    TECHNICAL FIELD
  • The present invention relates to a manufacturing method of a grain-oriented electrical steel sheet suitable for an iron core of a transformer (trans.) or the like.
  • BACKGROUND ART
  • A grain-oriented electrical steel sheet is a steel sheet which contains Si and in which crystal grains are highly integrated in a {110}<001> orientation (Goss orientation), and is used as a material of an iron core of a stationary induction device such as a transformer or the like. The control of the orientation of crystal grains is conducted with catastrophic grain growth phenomenon called secondary recrystallization.
  • As a method of controlling the secondary recrystallization, the following two methods can be cited. In one method, a slab is heated at a temperature of 1300°C or higher to solid-dissolve fine precipitates called inhibitors almost completely, and thereafter, is subjected to hot-rolling, cold-rolling, annealing, and so on, to cause fine precipitates to precipitate during the hot-rolling and the annealing. In the other method, a slab is heated at a temperature of lower than 1300°C, and thereafter, is subjected to hot-rolling, cold-rolling, decarburization annealing, a nitridation treatment, finish annealing, and so on, to cause AlN, (Al, Si)N, and so on to precipitate as an inhibitor during the nitridation treatment. The former method is sometimes called high-temperature slab heating, and the latter method is sometimes called low-temperature slab heating or intermediate-temperature slab heating.
  • Further, a material of iron core strongly requires a low core loss property in order to decrease loss to be caused during energy conversion. A core loss of a grain-oriented electrical steel sheet is classified into a hysteresis loss and an eddy current loss roughly. The hysteresis loss is affected by a crystal orientation, a defect, a grain boundary, and so on. The eddy current loss is affected by a thickness, an electrical resistance value, a 180-degree magnetic domain width, and so on.
  • Then, in recent years, in order to decrease the core loss drastically, there has been proposed a technique in which in order to drastically decrease the eddy current loss, which occupies most of the core loss, a groove and/or a strain are/is artificially introduced into the surface of a grain-oriented electrical steel sheet and further a 180-degree magnetic domain is subdivided. However, for the artificial introduction of a groove and/or a strain, man hours and cost for it are needed.
  • Further, there also has been proposed a technique regarding adjustment of annealing conditions and the like, but it has been difficult to sufficiently improve the core loss so far.
  • EP 2 418 294 A1 discloses a method for producing an electromagnetic steel sheet wherein the surface temperature of the slab at the start of a continuous casting step and a slab reheating step is specified.
  • CITATION LIST PATENT LITERATURE
    • Patent Literature 1: Japanese Laid-open Patent Publication No. 9-104922
    • Patent Literature 2: Japanese Laid-open Patent Publication No. 9-104923
    • Patent Literature 3: Japanese Examined Patent Application Publication No. 6-51887
    SUMMARY OF INVENTION TECHNICAL PROBLEM
  • The present invention has an object to provide a manufacturing method of a grain-oriented electrical steel sheet allowing core loss to be improved effectively.
  • SOLUTION TO PROBLEM
  • The present inventors, as a result of repeated earnest examinations with the aim of solving the above-described problems, found that by forming a large number of nuclei of grains in the Goss orientation before occurrence of secondary recrystallization, the number of grains in the Goss orientation after the secondary recrystallization can be increased, and by such an increase in the number of grains in the Goss orientation, core loss can be improved and further variations in core loss can also be decreased. Further, the present inventors also found that for the formation of nuclei, adjusting ranges of a Sn content and a P content in particular and conditions of hot-rolled sheet annealing is effective.
  • The present invention has been made based on the above-described knowledge, and the gist thereof is as follows.
    1. (1) A manufacturing method of a grain-oriented electrical steel sheet includes:
      • performing hot rolling of a slab containing, in mass%, C: 0.025% to 0.075%, Si: 2.5% to 4.0%, Mn: 0.03% to 0.30%, acid-soluble Al: 0.010% to 0.060%, N: 0.0010% to 0.0130%, Sn: 0.02% to 0.20%, S: 0.0010% to 0.020%, and P: 0.010% to 0.080%, optionally further containing at least one selected from the group consisting of, in mass%, Cr: 0.002% to 0.20%, Sb: 0.002% to 0.20%, Ni: 0.002% to 0.20%, Cu: 0.002% to 0.40%, Se: 0.0005% to 0.02%, Bi: 0.0005% to 0.02%, Pb: 0.0005% to 0.02%, B: 0.0005% to 0.02%, V: 0.002% to 0.02%, Mo: 0.002% to 0.02%, and As: 0.0005% to 0.02%, and a balance being composed of Fe and inevitable impurities to obtain a hot-rolled steel sheet;
      • performing hot-rolled sheet annealing of the hot-rolled steel sheet more than once to obtain an annealed steel sheet while intermediate annealing is performed therebetween at a temperature of 750°C to 1200°C for 30 seconds to 10 minutes;
      • performing cold rolling of the annealed steel sheet to obtain a cold-rolled steel sheet;
      • performing decarburization annealing of the cold-rolled steel sheet to obtain a decarburization-annealed steel sheet in which primary recrystallization has been caused;
      • finish annealing the decarburization-annealed steel sheet to make secondary recrystallization occur; and
      • further performing a nitridation treatment in which an N content of the decarburization-annealed steel sheet is increased, between beginning of the decarburization annealing and occurrence of the secondary recrystallization in the finish annealing, wherein
      • a finishing temperature in the hot rolling is 950°C or lower,
      • the hot-rolled sheet annealing is performed at 800°C to 1200°C,
      • a cooling rate from 750°C to 300°C in the hot-rolled sheet annealing is 10°C/second to 300°C/second, and
      • a reduction ratio in the cold rolling is 85% or more.
    2. (2) The manufacturing method of the grain-oriented electrical steel sheet according to (1), wherein the reduction ratio in the cold rolling is 88% or more.
    3. (3) The manufacturing method of the grain-oriented electrical steel sheet according to (1) or (2), wherein the reduction ratio in the cold rolling is 92% or less.
    4. (4) The manufacturing method of the grain-oriented electrical steel sheet according to any one of (1) to (3), wherein at least one pass in the cold rolling is performed at 200°C to 300°C.
    5. (5) The manufacturing method of the grain-oriented electrical steel sheet according to any one of (1) to (4), wherein an increasing temperature rate in the decarburization annealing is 30°C/second or more.
    6. (6) The manufacturing method of the grain-oriented electrical steel sheet according to any one of (1) to (5), wherein the slab further contains at least one selected from the group consisting of, in mass%, Cr: 0.002% to 0.20%, Sb: 0.002% to 0.20%, Ni: 0.002% to 0.20%, Cu: 0.002% to 0.40%, Se: 0.0005% to 0.02%, Bi: 0.0005% to 0.02%, Pb: 0.0005% to 0.02%, B: 0.0005% to 0.02%, V: 0.002% to 0.02%, Mo: 0.002% to 0.02%, and As: 0.0005% to 0.02%.
    ADVANTAGEOUS EFFECTS OF INVENTION
  • According to the present invention, composition of a slab, conditions of hot-rolled sheet annealing and so on are made appropriate, and thereby it is possible to improve core loss effectively without performing control of magnetic domains and so on.
  • BRIEF DESCRIPTION OF DRAWINGS
  • [Fig. 1] Fig. 1 is a flowchart illustrating a manufacturing method of a grain-oriented electrical steel sheet according to an embodiment of the present invention.
  • DESCRIPTION OF EMBODIMENTS
  • As described above, present inventors found that the formation of a large number of nuclei of grains in the Goss orientation before occurrence of secondary recrystallization contributes to improvement of core loss and a decrease in variations in core loss, and that, for the formation of nuclei, adjusting ranges of a Sn content and a P content in particular and conditions of hot-rolled sheet annealing are effective.
  • Hereinafter, there will be explained an embodiment of the present invention made based on these pieces of knowledge. Fig. 1 is a flowchart illustrating a manufacturing method of a grain-oriented electrical steel sheet according to the embodiment of the present invention. Hereinafter, % being the unit of the content of each component means mass%.
  • In the present embodiment, first, casting of a molten steel for a grain-oriented electrical steel sheet having a predetermined composition is performed to make a slab (Step S1). A method of casting is not limited in particular. The molten steel contains, for example, C: 0.025% to 0.075%, Si: 2.5% to 4.0%, Mn: 0.03% to 0.30%, acid-soluble Al: 0.010% to 0.060%, N: 0.0010% to 0.0130%, Sn: 0.02% to 0.20%, S: 0.0010% to 0.020%, and P: 0.010% to 0.080%. The balance of the molten steel is Fe and inevitable impurities. Incidentally, elements that form inhibitors in processes of manufacturing the grain-oriented electrical steel sheet and remain in the grain-oriented electrical steel sheet after purification by high-temperature annealing are also included in the inevitable impurities.
  • Here, there will be explained reasons for limiting the numerical values of the composition of the above-described molten steel.
  • C is an element effective for controlling a structure obtained through primary recrystallization (primary recrystallization structure). When the C content is less than 0.025%, this effect cannot be obtained sufficiently. On the other hand, when the C content exceeds 0.075%, time required for decarburization annealing is long, which results in increasing an amount of CO2 emissions. Incidentally, unless the decarburization annealing is performed sufficiently, a grain-oriented electrical steel sheet having a good magnetic property is not easily obtained. Thus, the C content is set to 0.025% to 0.075%.
  • Si is an element quite effective for increasing electrical resistance of a grain-oriented electrical steel sheet to thereby decrease an eddy current loss constituting a part of a core loss. When the Si content is less than 2.5%, it is not possible to sufficiently suppress the eddy current loss. On the other hand, when the Si content exceeds 4.0%, cold working is difficult to be performed. Thus, the Si content is set to 2.5% to 4.0%.
  • Mn increases specific resistance of a grain-oriented electrical steel sheet to decrease a core loss. Mn also exhibits a function of preventing occurrence of crack during hot rolling. When the Mn content is less than 0.03%, these effects cannot be obtained sufficiently. On the other hand, when the Mn content exceeds 0.30%, a magnetic flux density of a grain-oriented electrical steel sheet decreases. Thus, the Mn content is set to 0.03% to 0.30%.
  • Acid-soluble Al is an important element which forms AlN functioning as an inhibitor. When the content of acid-soluble Al is less than 0.010%, it is not possible to form a sufficient amount of AlN and thus inhibitor strength is insufficient. On the other hand, when the content of acid-soluble Al exceeds 0.060%, AlN coarsens, and thereby the inhibitor strength decreases. Thus, the content of acid-soluble Al is set to 0.010% to 0.060%.
  • N is an important element that reacts with acid-soluble Al to thereby form AlN. As will be described later, a nitridation treatment is performed after cold rolling, so that a large amount of N is not required to be contained in a steel for a grain-oriented electrical steel sheet, but when the N content is set to be less than 0.0010%, there is sometimes a case that a large load is required during manufacturing a steel. On the other hand, when the N content exceeds 0.0130%, a hole called blister is caused in a steel sheet during cold rolling. Thus, the N content is set to 0.0010% to 0.0130%.
  • Sn contributes to the formation of nuclei of grains in the Goss orientation. Though details of the reason are unclear, it is inferably because by the addition of Sn, a slip system of Fe changes and a deformation style in deformation by rolling differs from the case of no Sn being added. Further, Sn improves the quality of an oxide layer formed during decarburization annealing, and also improves the quality of a glass film formed using the oxide layer during finish annealing. That is, Sn improves the magnetic property and suppresses variations in magnetic property, through the stabilization of formation of the oxide layer and the glass film. When the Sn content is less than 0.02%, these effects cannot be obtained sufficiently. On the other hand, when the Sn content exceeds 0.20%, there is sometimes a case that a surface of a steel sheet is difficult to be oxidized and thus the formation of a glass film is insufficient. Thus, the Sn content is set to 0.02% to 0.20%.
  • S is an important element that reacts with Mn to thereby form MnS precipitates. The MnS precipitates mainly affect the primary recrystallization to exhibit a function of suppressing locational variation in grain growth of the primary recrystallization due to the hot rolling. When the S content is less than 0.0010%, this effect cannot be obtained sufficiently. On the other hand, when the S content exceeds 0.020%, the magnetic property is likely to deteriorate. Thus, the S content is set to 0.0010% to 0.020%.
  • P increases the specific resistance of a grain-oriented electrical steel sheet to decrease a core loss. Further, P contributes to the formation of nuclei of grains in the Goss orientation. Though details of this reason are unclear, similarly to Sn, it is inferably because by the addition of P, a slip system of Fe changes and a deformation style in deformation by rolling differs from the case of no P being added. When the P content is less than 0.010%, these effects cannot be obtained sufficiently. On the other hand, when the P content exceeds 0.080%, the cold rolling sometimes is difficult to be performed. Thus, the P content is set to 0.010% to 0.080%.
  • Note that at least one of the following various elements may also be contained in the molten steel.
  • Cr improves the quality of an oxide layer formed during decarburization annealing, and also improves the quality of a glass film formed using the oxide layer during finish annealing. That is, Cr improves the magnetic property and suppresses variations in magnetic property, through the stabilization of formation of the oxide layer and the glass film. However, when the Cr content exceeds 0.20%, there is sometimes a case that the formation of a glass film is unstable. Thus, the Cr content is preferably 0.20% or less. Further, in order to sufficiently obtain the above-described effects, the Cr content is preferably 0.002% or more.
  • Further, the molten steel may also contain at least one selected from the group consisting of Sb: 0.002% to 0.20%, Ni: 0.002% to 0.20%, Cu: 0.002% to 0.40%, Se: 0.0005% to 0.02%, Bi: 0.0005% to 0.02%, Pb: 0.0005% to 0.02%, B: 0.0005% to 0.02%, V: 0.002% to 0.02%, Mo: 0.002% to 0.02%, and As: 0.0005% to 0.02%. Each of these elements is an inhibitor strengthening element.
  • In the present embodiment, after the slab is made from the molten steel having such a composition, the slab is heated (Step S2). The temperature of the heating is preferably set to 1250°C or lower from the viewpoint of energy saving.
  • Then, the hot rolling of the slab is performed to thereby obtain a hot-rolled steel sheet (Step S3). In the present embodiment, a finishing temperature of the hot rolling is set to 950°C or lower. When the finishing temperature is higher than 950°C, a texture deteriorates in the subsequent processes and particularly the nuclei of grains in the Goss orientation, which are formed during decarburization annealing, are decreased. Incidentally, the thickness of a hot-rolled steel sheet is not limited in particular, and is set to 1.8 mm to 3.5 mm, for example.
  • Thereafter, hot-rolled sheet annealing of the hot-rolled steel sheet is performed to thereby obtain an annealed steel sheet (Step S4). In the present embodiment, the hot-rolled sheet annealing is performed at 800°C to 1200°C. When the temperature of the hot-rolled sheet annealing is lower than 800°C, recrystallization of the hot-rolled steel sheet (hot-rolled sheet) is insufficient and a texture after the cold rolling and the subsequent decarburization annealing deteriorates to thereby make it difficult to obtain a grain-oriented electrical steel sheet provided with a sufficient magnetic property. On the other hand, when the temperature of the hot-rolled sheet annealing is higher than 1200°C, brittle deterioration of the hot-rolled steel sheet (hot-rolled sheet) is significant to increase a possibility that fracture is caused in the subsequent cold rolling. Further, in the present embodiment, in cooling from 800°C to 1200°C, a cooling rate from 750°C to 300°C is set to 10°C /second to 300°C /second. When the cooling rate in the temperature range is less than 10°C/second, a texture after the cold rolling and the subsequent decarburization annealing deteriorates to thereby make it difficult to obtain a grain-oriented electrical steel sheet provided with a sufficient magnetic property. On the other hand, when the cooling rate in the temperature range is greater than 300°C/second, a cooling facility is likely to be overloaded. Incidentally, the cooling rate in the temperature range is preferably set to 20°C/second or more.
  • Subsequently, the cold rolling of the annealed steel sheet is performed to thereby obtain a cold-rolled steel sheet (Step S5). The cold rolling is performed a plurality of times while intermediate annealing being performed therebetween. The intermediate annealing is performed at a temperature of 750°C to 1200°C for 30 seconds to 10 minutes.
  • Incidentally, when the cold rolling is performed without the intermediate annealing as described above being performed, there is sometimes a case that a uniform property is not easily obtained. Meanwhile, when the cold rolling is performed a plurality of times while the intermediate annealing being performed therebetween, a uniform property is easily obtained, but the magnetic flux density sometimes decreases. Thus, the number of times of the cold rolling and whether or not the intermediate annealing is performed are preferably determined according to the property and cost required for a grain-oriented electrical steel sheet to be obtained finally.
  • Further, even in any case, a reduction ratio in the cold rolling is set to 85% or more. When the reduction ratio is less than 85%, grains in orientations deviated from the Goss orientation are generated in the subsequent secondary recrystallization. Further, in order to obtain a better property, the reduction ratio is preferably set to 88% or more. Further, the reduction ratio is preferably set to 92% or less. When the reduction ratio is greater than 92%, similarly to the case of being less than 85%, grains deviated from the Goss orientation are generated in the subsequent secondary recrystallization.
  • After the cold rolling, the decarburization annealing is performed on the cold-rolled steel sheet in a moist atmosphere containing hydrogen and nitrogen, to thereby obtain a decarburization-annealed steel sheet (Step S6). Carbon in the steel sheet is removed by the decarburization annealing, and the primary recrystallization occurs. The temperature of the decarburization annealing is not limited in particular, but when the temperature of the decarburization annealing, is lower than 800°C, grains obtained by the primary recrystallization (primary recrystallization grains) may be too small, and thus there is sometimes a case that the subsequent secondary recrystallization does not sufficiently occur. On the other hand, when the temperature of the decarburization annealing exceeds 950°C, the primary recrystallization grains may be too large, and thus there is sometimes a case that the subsequent secondary recrystallization does not sufficiently occur.
  • Thereafter, an annealing separating agent containing MgO as its main component in a water slurry form is applied on the surface of the decarburization-annealed steel sheet, and the decarburization-annealed steel sheet is coiled. Then, batch-type finish annealing is performed on the coiled decarburization-annealed steel sheet to thereby obtain a coiled finish-annealed steel sheet (Step S8). The secondary recrystallization occurs through the finish annealing.
  • Further, the nitridation treatment is performed between beginning of the decarburization annealing and occurrence of the secondary recrystallization in the finish annealing (Step S7). This is to form inhibitors of (Al, Si)N. The above nitridation treatment may be performed during the decarburization annealing (Step S6), or may also be performed during the finish annealing (Step S8). In the case when it is performed during the decarburization annealing, the annealing may be performed in an atmosphere containing a gas having nitriding capability such as ammonia, for example. Meanwhild, the nitridation treatment may be performed at a heating zone or a soaking zone in a continuous annealing furnace, or the nitridation treatment may also be performed at a stage after the soaking zone. In the case when the nitridation treatment is performed during the finish annealing, a powder having nitriding capability such as MnN, for example, may be added to the annealing separating agent.
  • Then, after the finish annealing, the coiled finish-annealed steel sheet is uncoiled, and the annealing separating agent is removed. Subsequently, a coating solution containing aluminum phosphate and colloidal silica as its main component is applied on the surface of the finish-annealed steel sheet and is baked to form an insulating film (Step S9).
  • The grain-oriented electrical steel sheet can be manufactured as described above.
  • It should be noted that the above-described embodiment merely illustrates a concrete example of implementing the present invention, and the technical scope of the present invention is not to be construed in a restrictive manner by the embodiment. That is, the present invention may be implemented in various forms without departing from the technical spirit or main features thereof.
  • [Reference Example]
  • Next, experiments conducted by the present inventors will be explained. "Example" in this section means "reference example". Conditions and so on in these experiments are examples employed for confirming the applicability and effects disclosed in the present application, and the present invention is not limited to these examples.
  • (Experiment 1)
  • In Experiment 1, first, in a vacuum melting furnace, 13 types of steel ingots were made each containing, in mass%, Si: 3.2%, C: 0.05%, Mn: 0.1%, Al: 0.03%, N: 0.01%, S: 0.01%, Cu: 0.02%, Ni: 0.02%, and As: 0.001%, and further containing Sn and P at various content. The balance of each of the steel ingots was Fe and inevitable impurities. The Sn content and the P content of each of the steel ingots are listed in Table 1. Then, on each of the steel ingots, annealing was performed at 1150°C for one hour and thereafter hot rolling was performed, to thereby obtain hot-rolled steel sheets (hot-rolled sheets) each having a thickness of 2.3 mm. A finishing temperature of the hot rolling was set to 940°C.
  • Subsequently, annealing was performed on each of the hot-rolled sheets at 1100°C for 120 seconds, and thereafter the hot-rolled sheets were each soaked in a hot water bath to be cooled at a cooling rate of 35°C/s from 750°C to 300°C. Then, pickling was performed, and thereafter cold rolling was performed to thereby obtain cold-rolled steel sheets (cold-rolled sheets) each having a thickness of 0.23 mm. In the cold rolling, the rolling was performed by about 30 passes, and at two passes out of them, the hot-rolled sheets were each heated to 250°C to be subjected to the rolling immediately. Subsequently, on each of the cold-rolled sheets, decarburization annealing was performed at 860°C for 100 seconds in a gas atmosphere containing water vapor, hydrogen, and nitrogen, and subsequently nitridation annealing was performed at 770°C for 20 seconds in a gas atmosphere containing hydrogen, nitrogen, and ammonia. An increasing temperature rate in the decarburization annealing was set to 32°C/s. Then, an annealing separating agent containing MgO as its main component in a water slurry form was applied, and then finish annealing was performed at 1200°C for 20 hours.
  • Finish-annealed steel sheets were each water washed, and of each of the steel sheets, a single-sheet for magnetic measurement having a size of W60 × L300 mm was cut out. Then, application and baking of a coating solution containing aluminum phosphate and colloidal silica as its main component were performed. Thus, grain-oriented electrical steel sheets each having an insulating film attached thereto were manufactured.
  • Then, annealing of each of the manufactured grain-oriented electrical steel sheets was performed at 750°C for two hours to thereby, remove a strain (for example, a shear strain) caused when cutting out. Thereafter, a core loss W17/50 was measured. At that time, under each of 13 types of conditions, the measurement of the core loss W17/50 was performed on the five single-sheets and an average value (average W17/50) and a difference between a maximum value and a minimum value (ΔW17/50) of measurement results were calculated. This result is listed in Table 1. Incidentally, the core loss W17/50 is the value of core loss obtained when the magnetic flux density of 1.7 T is applied at 50 Hz. Further, the difference between the maximum value and the minimum value is the index indicating variations in the core loss W17/50.
  • [Table 1]
  • TABLE 1
    SYMBOL No. Sn(%) P(%) AVERAGE W17/50 (W/kg) Δ W17/50 (W/kg) REMARK
    1-1 0.004 0.007 0.876 0.264 COMPARATIVE EXAPLE
    1-2 0.005 0.028 0.867 0.223 COMPARATIVE EXAPLE
    1-3 0.02 0.027 0.848 0.162 EXAMPLE
    1-4 0.06 0.026 0.821 0.091 EXAMPLE
    1-5 0.12 0.028 0.825 0.084 EXAMPLE
    1-6 0.19 0.026 0.838 0.073 EXAMPLE
    1-7 0.22 0.027 0.862 0.061 COMPARATIVE EXAPLE
    1-8 0.04 0.007 0.863 0.224 COMPARATIVE EXAPLE
    1-9 0.04 0.011 0.849 0.164 EXAMPLE
    1-10 0.04 0.024 0.822 0.093 EXAMPLE
    1-11 0.05 0.047 0.826 0.081 EXAMPLE
    1-12 0.05 0.078 0.839 0.072 EXAMPLE
    1-13 0.04 0.085 IMPOSSIBLE TO MEASURE MAGNETIC CHARACTERISTICS COMPARATIVE EXAPLE
  • As listed in Table 1, in symbols No. 1-3 to No. 1-6 and No. 1-9 to No. 1-12 each having the Sn content of 0.02% to 0.20% and the P content of 0.010% to 0.080%, the average W17/50 was 0.85 W/kg or less, which was small, and ΔW17/50 was also 0.2 W/kg or less, which was small. That is, in the symbols No. 1-3 to No. 1-6 and No. 1-9 to No. 1-12, it was possible to obtain the good magnetic property. In the symbols No. 1-4, No. 1-5, No. 1-10, and No. 1-11, which were particularly good among them, the Sn content was 0.04% to 0.12% and the P content was 0.020% to 0.050%. Incidentally, in a symbol No. 1-13, fracture was caused in the cold rolling, and thus it was not possible to manufacture a grain-oriented electrical steel sheet.
  • (Experiment 2)
  • In Experiment 2, first, in a vacuum melting furnace, steel ingots were made each containing, in mass%, Si: 3.2%, C: 0.06%, Mn: 0.1%, Al: 0.03%, N: 0.01%, S: 0.01%, Sn: 0.04%, P: 0.03%, Sb: 0.02%, Cr: 0.09%, and Pb: 0.001%. The balance of each of the steel ingots was Fe and inevitable impurities. Then, on each of the steel ingots, annealing was performed at 1180°C for one hour and thereafter hot rolling was performed, to thereby obtain hot-rolled steel sheets (hot-rolled sheets) each having a thickness of 2.3 mm. Between the annealing and the hot rolling, waiting was performed for various time periods, and a finishing temperature (FT) of the hot rolling was varied between 880°C and 970°C. The finishing temperature (FT) is listed in Table 2.
  • Subsequently, hot-rolled sheet annealing was performed on each of the hot-rolled sheets at an annealing temperature (HA) between 780°C and 1210°C for 110 seconds, and then the hot-rolled sheets were each cooled. At that time, a cooling method was changed and a cooling rate (CR) from 750°C to 300°C. was varied between 5°C/s and 295°C/s. As the cooling method, there can be cited air cooling, hot-water cooling using water at 100°C, hot-water cooling using water at 80°C, hot-water cooling using water at 70°C, hot-water cooling using water at 60°C, hot-water cooling using water at 40°C, water cooling (20°C) using water at 20°C, and ice salt-water cooling using ice salt water. The annealing temperature (HA) and the cooling rate (CR) of each of the hot-rolled sheets are listed in Table 2. Thereafter, cold rolling was performed to thereby obtain cold-rolled steel sheets (cold-rolled sheets) each having a thickness of 0.23 mm. In the cold rolling, the rolling was performed by about 30 passes, and at two passes out of them, the hot-rolled sheets were each heated to 250°C to be subjected to the rolling immediately. Subsequently, on each of the cold-rolled sheets, decarburization annealing was performed at 850°C for 90 seconds in a gas atmosphere containing water vapor, hydrogen, and nitrogen, and subsequently nitridation annealing was performed at 750°C for 20 seconds in a gas atmosphere containing hydrogen, nitrogen, and ammonia. An increasing temperature rate in the decarburization annealing was set to 33°C/s. Then, an annealing separating agent containing MgO as its main component in a water slurry form was applied, and then finish annealing was performed at 1200°C for 20 hours.
  • Finish-annealed steel sheets were each water washed, and of each of the steel sheets, a single-sheet for magnetic measurement having a size of W60 × L300 mm was cut out. Then, application and baking of a coating solution containing aluminum phosphate and colloidal silica as its main component were performed. Thus, grain-oriented electrical steel sheets each having an insulating film attached thereto were manufactured.
  • Then, by a method similar to that in Experiment 1, a value of the "average W17/50" and a value of "ΔW17/50" were obtained. This result is listed in Table 2.
  • [Table 2]
  • TABLE 2
    SYMBOL No. FT (°C) HA (°C) CR (°C/s) AVERAGE W17/50 (W/kg) ΔW17/50 (W/kg) REMARK
    2-1 880 1050 25 0.821 0.071 EXAMPLE
    2-2 920 1050 25 0.828 0.093 EXAMPLE
    2-3 940 1050 25 0.834 0.139 EXAMPLE
    2-4 970 1050 25 0.853 0.224 COMPARATIVE EXAPLE
    2-5 930 780 45 0.872 0.258 COMPARATIVE EXAPLE
    2-6 930 810 45 0.847 0.188 EXAMPLE
    2-7 930 910 45 0.843 0.173 EXAMPLE
    2-8 930 1010 45 0.838 0.158 EXAMPLE
    2-9 930 1110 45 0.822 0.093 EXAMPLE
    2-10 930 1210 45 IMPOSSIBLE TO MEASURE MAGNETIC CHARACTERISTICS COMPARATIVE EXAPLE
    2-11 930 1100 5 0.864 0.254 COMPARATIVE EXAPLE
    2-12 930 1100 13 0.828 0.164 EXAMPLE
    2-13 930 1100 29 0.821 0.092 EXAMPLE
    2-14 930 1100 95 0.839 0.081 EXAMPLE
    2-15 930 1100 196 0.842 0.072 EXAMPLE
    2-16 930 1100 295 0.848 0.063 EXAMPLE
  • As listed in Table 2, in symbols No. 2-1 to No. 2-3, No. 2-6 to No. 2-9, and No. 2-12 to No. 2-16 each having the finishing temperature (FT) of 950°C or lower, the annealing temperature (HA) of 800°C to 1200°C, and the cooling rate (CR) of 10°C/s to 300°C/s, the average W17/50 was 0.85 W/kg or less, which was small, and ΔW17/50 was also 0.2 W/kg or less, which was small. That is, in the symbols No. 2-1 to No. 2-3, No. 2-6 to No. 2-9, and No. 2-12 to No. 2-16, it was possible to obtain the good magnetic property. In the symbols No. 2-1, No. 2-2, No. 2-9, No. 2-12, and No. 2-13, which were particularly good out of them, the finishing temperature (FT) was 930°C or lower, the annealing temperature (HA) was 1050°C to 1200°C, and the cooling rate (CR) was 10°C/s to 50°C/s. Incidentally, in a symbol No. 2-10, the annealing temperature (HA) was 1210°C, which was high, and the brittle deterioration was severe. Then, it was not possible to manufacture a grain-oriented electrical steel sheet because fracture was caused in the cold rolling.
  • (Experiment 3)
  • In Experiment 3, first, in a vacuum melting furnace, steel ingots were made each containing, in mass%, Si: 3.1%, C: 0.04%, Mn: 0.1%, Al: 0.03%, N: 0.01%, S: 0.01%, Sn: 0.06%, P: 0.02%, Se: 0.001%, V: 0.003%, As: 0.001%, Mo: 0.002%, and Bi: 0.001%. The balance of each of the steel ingots is Fe; and inevitable impurities. Then, on each of the steel ingots, annealing was performed at 1150°C for one hour and thereafter hot rolling was performed, to thereby obtain hot-rolled steel sheets (hot-rolled sheets) having various thicknesses (HG). The thickness of each of the hot-rolled sheets (HG) is listed in Table 3. A finishing temperature of the hot rolling was set to 940°C.
  • Subsequently, on each of the hot-rolled sheets, annealing was performed at 1120°C for 10 seconds and further annealing was performed at 920°C for 100 seconds, and thereafter the hot-rolled sheets were each soaked in a hot water bath to be cooled at a cooling rate of 25°C/s from 750°C to 300°C. Then, pickling was performed, and thereafter cold rolling was performed to thereby obtain cold-rolled steel sheets (cold-rolled sheets) each having a thickness of 0.275 mm. In the cold rolling, the rolling was performed by 30 to 40 passes, and at one pass out of them, the hot-rolled sheets were each heated to 240°C to be subjected to the rolling immediately. As for the four steel sheets, the heating to 240°C was omitted. Whether or not the heating was performed is listed in Table 3. Subsequently, on each of the cold-rolled sheets, decarburization annealing was performed at 850°C for 110 seconds in a gas atmosphere containing water vapor, hydrogen, and nitrogen, and subsequently nitridation annealing was performed at 750°C for 20 seconds in a gas atmosphere containing hydrogen, nitrogen, and ammonia. An increasing temperature rate in the decarburization annealing was set to 31°C/s. Then, an annealing separating agent containing MgO as its main component in a water slurry form was applied, and then finish annealing was performed at 1180°C for 20 hours.
  • Finish-annealed steel sheets were each water washed, and of each of the steel sheets, a single-sheet for magnetic measurement having a size of W60 × L300 mm was cut out. Then, application and baking of a coating solution containing aluminum phosphate and colloidal silica as its main component were performed. Thus, grain-oriented electrical steel sheets each having an insulating film attached thereto were manufactured.
  • Then, by a method similar to that in Experiment 1, a value of the "average W17/50" and a value of "ΔW17/50" were obtained. This result is listed in Table 3. Incidentally, the cold-rolling ratio in Table 3 is a value obtained from the thickness of the hot-rolled sheet (HG) and the thickness of the cold-rolled sheet (0.275 mm).
  • [Table 3]
  • TABLE 3
    SYMBOL No. HG (mm) REDUCTION RATIO (%) WITH OR WITHOUT HEATING AVERATE W17/50 (W/kg) ΔW17/50 (W/kg) REMARK
    3-1 1.72 84 WITH 0.977 0.086 COMPARATIVE EXAPLE
    3-2 1.83 85 WITH 0.929 0.092 EXAMPLE
    3-3 1.96 86 WITH 0.924 0.097 EXAMPLE
    3-4 2.29 88 WITH 0.909 0.104 EXAMPLE
    3-5 2.29 88 WITHOUT 0.968 0.203 COMPARATIVE EXAPLE
    3-6 2.75 90 WITH 0.888 0.121 EXAMPLE
    3-7 2.75 90 WITHOUT 0.947 0.224 COMPARATIVE EXAPLE
    3-8 3.06 91 WITH 0.886 0.146 EXAMPLE
    3-9 3.06 91 WITHOUT 0.945 0.247 COMPARATIVE EXAPLE
    3-10 3.44 92 WITH 0.903 0.188 EXAMPLE
    3-11 3.44 92 WITHOUT 0.941 0.287 COMPARATIVE EXAPLE
    3-12 3.93 93 WITH 0.952 0.259 COMPARATIVE EXAPLE
  • As listed in Table 3, in symbols No. 3-2 to No. 3-4, No. 3-6, No. 3-8, and No. 3-10 each having the cold-rolling ratio of 85% to 92% and having the heating to 240°C performed thereon, the average W17/50 was 0.93 W/kg or less, which was small, and ΔW17/50 was also 0.2 W/kg or less, which was small. That is, in the symbols No. 3-2 to No. 3-4, No. 3-6, No. 3-8, and No. 3-10, it was possible to obtain the good magnetic property. In the symbols No. 3-4, No. 3-6, No. 3-8, and No. 3-10 each having the average W17/50 of 0.91 W/kg or less, which were particularly good among them, the cold-rolling ratio was 88% to 92% and the heating to 240°C was performed.
  • (Experiment 4)
  • In Experiment 4, first, in a vacuum melting furnace, three types of steel ingots were made each containing, in mass%, Si: 3.1%, C: 0.07%, Mn: 0.1%, Al: 0.03%, N: 0.01%, S: 0.01%, Cu: 0.09%, and B: 0.001%, and further containing Sn and P at various content. The balance of each of the steel ingots was Fe and inevitable impurities. The Sn content and the P content of each of the steel ingots are listed in Table 4. Then, on each of the steel ingots, annealing was performed at 1150°C for one hour and thereafter hot rolling was performed, to thereby obtain hot-rolled steel sheets (hot-rolled sheets) each having a thickness of 2.5 mm. A finishing temperature of the hot rolling was set to 930°C.
  • Subsequently, on each of the hot-rolled sheets, annealing was performed at 1080°C for 110 seconds, and thereafter the hot-rolled sheets were each soaked in a hot water bath to be cooled at a cooling rate of 32°C/s from 750°C to 300°C. Then, pickling was performed, and thereafter cold rolling was performed to thereby obtain cold-rolled steel sheets (cold-rolled sheets) each having a thickness of 0.230 mm. In the cold rolling, the rolling was performed by about 30 passes, and at one pass out of them, the hot-rolled sheets were each heated to 270°C to be subjected to the rolling immediately. Subsequently, on each of the cold-rolled sheets, decarburization annealing was performed at 830°C for 80 seconds in a gas atmosphere containing water vapor, hydrogen, and nitrogen, and subsequently nitridation annealing was performed at 800°C for 30 seconds in a gas atmosphere containing hydrogen, nitrogen, and ammonia. An increasing temperature rate (HR) in the decarburization annealing was varied between 15°C/s and 300°C/s. The increasing temperature rate (HR) is listed in Table 4. Then, an annealing separating agent containing MgO as its main component in a water slurry form was applied, and then finish annealing was performed at 1190°C for 20 hours.
  • Finish-annealed steel sheets were each water washed, and of each of the steel sheets, a single-sheet for magnetic measurement having a size of W60 × L300 mm was cut out. Then, application and baking of a coating solution containing aluminum phosphate and colloidal silica as its main component were performed. Thus, grain-oriented electrical steel sheets each having an insulating film attached thereto were manufactured.
  • Then, by a method similar to that in Experiment 1, a value of the "average W17/50" and a value of "ΔW17/50" were obtained. This result is listed in Table 4.
  • [Table 4]
  • TABLE 4
    SYMBOL No. Sn P HR AVERAGE W17/50 (W/kg) ΔW17/50 (W/kg) REMARK
    4-1 0.004 0.007 15 0.897 0.328 COMPARATIVE EXAPLE
    4-2 35 0.868 0.254 COMPARATIVE EXAPLE
    4-3 100 0.846 0.223 COMPARATIVE EXAPLE
    4-4 300 0.849 0.211 COMPARATIVE EXAPLE
    4-5 0.08 0.031 15 0.838 0.189 EXAMPLE
    4-6 35 0.824 0.122 EXAMPLE
    4-7 100 0.811 0.083 EXAMPLE
    4-8 300 0.814 0.079 EXAMPLE
    4-9 0.22 0.055 15 0.919 0.137 COMPARATIVE EXAPLE
    4-10 35 0.904 0.082 COMPARATIVE EXAPLE
    4-11 100 0.893 0.074 COMPARATIVE EXAPLE
    4-12 300 0.898 0.063 COMPARATIVE EXAPLE
  • As listed in Table 4, in symbols No. 4-5 to No. 4-8 each having the Sn content of 0.02% to 0.20% and the P content of 0.010% to 0.080%, the average W17/50 was 0.85 W/kg or less, which was small, and ΔW17/50 was also 0.20 W/kg or less, which was small. That is, in the symbols No. 4-5 to No. 4-8, it was possible to obtain the good magnetic property. In the symbols No. 4-6 to No. 4-8 each having the average W17/50 of 0.83 W/kg or less and ΔW17/50 of 0.15 W/kg or less, which were particularly good among them, the increasing temperature rate (HR) was 30°C/s or more.
  • INDUSTRIAL APPLICABILITY
  • The present invention may be utilized in an industry of manufacturing electrical steel sheets and an industry of utilizing electrical steel sheets, for example.

Claims (6)

  1. A manufacturing method of a grain-oriented electrical steel sheet comprising:
    performing hot rolling of a slab containing, in mass%, C: 0.025% to 0.075%, Si: 2.5% to 4.0%, Mn: 0.03% to 0.30%, acid-soluble Al: 0.010% to 0.060%, N: 0.0010% to 0.0130%, Sn: 0.02% to 0.20%, S: 0.0010% to 0.020%, and P: 0.010% to 0.080%, optionally further containing at least one selected from the group consisting of, in mass%, Cr: 0.002% to 0.20%, Sb: 0.002% to 0.20%, Ni: 0.002% to 0.20%, Cu: 0.002% to 0.40%, Se: 0.0005% to 0.02%, Bi: 0.0005% to 0.02%, Pb: 0.0005% to 0.02%, B: 0.0005% to 0.02%, V: 0.002% to 0.02%, Mo: 0.002% to 0.02%, and As: 0.0005% to 0.02%, and a balance being composed of Fe and inevitable impurities to obtain a hot-rolled steel sheet;
    performing hot-rolled sheet annealing of the hot-rolled steel sheet to obtain an annealed steel sheet;
    performing cold rolling of the annealed steel sheet more than once to obtain a cold-rolled steel sheet while intermediate annealing is performed therebetween at a temperature of 750°C to 1200°C for 30 seconds to 10 minutes;
    performing decarburization annealing of the cold-rolled steel sheet to obtain a decarburization-annealed steel sheet in which primary recrystallization has been caused;
    finish annealing the decarburization-annealed steel sheet to make secondary recrystallization occur; and
    further performing a nitridation treatment in which an N content of the decarburization-annealed steel sheet is increased, between beginning of the decarburization annealing and occurrence of the secondary recrystallization in the finish annealing, wherein
    a finishing temperature in the hot rolling is 950°C or lower,
    the hot-rolled sheet annealing is performed at 800°C to 1200°C,
    a cooling rate from 750°C to 300°C in the hot-rolled sheet annealing is 10°C/second to 300°C/second, and
    a reduction ratio in the cold rolling is 85% or more.
  2. The manufacturing method of the grain-oriented electrical steel sheet according to claim 1, wherein the reduction ratio in the cold rolling is 88% or more.
  3. The manufacturing method of the grain-oriented electrical steel sheet according to claim 1 or 2, wherein the reduction ratio in the cold rolling is 92% or less.
  4. The manufacturing method of the grain-oriented electrical steel sheet according to any one of claims 1 to 3, wherein at least one pass in the cold rolling is performed at 200°C to 300°C.
  5. The manufacturing method of the grain-oriented electrical steel sheet according to any one of claims 1 to 4, wherein an increasing temperature rate in the decarburization annealing is 30°C/second or more.
  6. The manufacturing method of the grain-oriented electrical steel sheet according to any one of claims 1 to 5, wherein the slab further contains at least one selected from the group consisting of, in mass%, Cr: 0.002% to 0.20%, Sb: 0.002% to 0.20%, Ni: 0.002% to 0.20%, Cu: 0.002% to 0.40%, Se: 0.0005% to 0.02%, Bi: 0.0005% to 0.02%, Pb: 0.0005% to 0.02%, B: 0.0005% to 0.02%, V: 0.002% to 0.02%, Mo: 0.002% to 0.02%, and As: 0.0005% to 0.02%.
EP12881480.3A 2012-07-20 2012-07-20 Manufacturing method of grain-oriented electrical steel sheet Active EP2876173B9 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
PL12881480T PL2876173T3 (en) 2012-07-20 2012-07-20 Manufacturing method of electrical steel sheet grain-oriented

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/JP2012/068483 WO2014013615A1 (en) 2012-07-20 2012-07-20 Process for producing grain-oriented electrical steel sheet

Publications (5)

Publication Number Publication Date
EP2876173A1 EP2876173A1 (en) 2015-05-27
EP2876173A4 EP2876173A4 (en) 2016-02-24
EP2876173B1 EP2876173B1 (en) 2018-10-24
EP2876173B8 EP2876173B8 (en) 2018-12-26
EP2876173B9 true EP2876173B9 (en) 2019-06-19

Family

ID=49948466

Family Applications (1)

Application Number Title Priority Date Filing Date
EP12881480.3A Active EP2876173B9 (en) 2012-07-20 2012-07-20 Manufacturing method of grain-oriented electrical steel sheet

Country Status (9)

Country Link
US (1) US20150170812A1 (en)
EP (1) EP2876173B9 (en)
JP (1) JP5423909B1 (en)
KR (1) KR20150007360A (en)
CN (1) CN103687966A (en)
BR (1) BR112013015997B1 (en)
PL (1) PL2876173T3 (en)
RU (1) RU2593051C1 (en)
WO (1) WO2014013615A1 (en)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20160108488A1 (en) * 2014-10-15 2016-04-21 Sms Siemag Ag Process for producing grain-oriented electrical steel strip and grain-oriented electrical steel strip obtained according to said process
RU2665649C1 (en) * 2014-11-27 2018-09-03 ДжФЕ СТИЛ КОРПОРЕЙШН Method of making plate of textured electrical steel
KR101633255B1 (en) 2014-12-18 2016-07-08 주식회사 포스코 Grain-orientied electrical shteel sheet and method for manufacturing the same
KR101664096B1 (en) * 2014-12-24 2016-10-10 주식회사 포스코 Grain-orientied electrical steel sheet and method for manufacturing the same
JP6485554B2 (en) * 2015-10-26 2019-03-20 新日鐵住金株式会社 Directional electrical steel sheet and method for producing the same, and method for producing decarburized steel sheet for directionally oriented electrical steel sheet
JP6836318B2 (en) * 2015-11-25 2021-02-24 日本製鉄株式会社 Directional electromagnetic steel sheet and its manufacturing method and heat-rolled sheet for grain-oriented electrical steel sheet and its manufacturing method
CN109983158A (en) 2016-10-31 2019-07-05 日本制铁株式会社 Grain-oriented magnetic steel sheet
RU2712795C1 (en) * 2016-11-25 2020-01-31 ДжФЕ СТИЛ КОРПОРЕЙШН Electrotechnical steel with non-oriented structure and method of its production
PL3569726T3 (en) * 2017-01-16 2022-08-01 Nippon Steel Corporation Non-oriented electrical steel sheet and method for manufacturing non-oriented electrical steel sheet
RU2637848C1 (en) * 2017-01-31 2017-12-07 Общество с ограниченной ответственностью "ВИЗ-Сталь" Method for producing high-permeability anisotropic electrical steel
KR102012319B1 (en) 2017-12-26 2019-08-20 주식회사 포스코 Oriented electrical steel sheet and manufacturing method of the same
JP7486436B2 (en) * 2019-01-16 2024-05-17 日本製鉄株式会社 Manufacturing method for grain-oriented electrical steel sheet
JP6856179B1 (en) * 2019-04-23 2021-04-07 Jfeスチール株式会社 Manufacturing method of grain-oriented electrical steel sheet
KR20240035910A (en) * 2019-04-23 2024-03-18 제이에프이 스틸 가부시키가이샤 Method for producing grain-oriented electrical steel sheet
WO2021054408A1 (en) * 2019-09-18 2021-03-25 日本製鉄株式会社 Method for manufacturing grain-oriented electrical steel sheet
CN112921152B (en) * 2021-02-01 2022-05-17 襄阳裕丰德科技有限公司 Novel heat treatment process for full-hardened cold-rolled working roll
CN115838845B (en) * 2022-10-20 2024-05-03 河南中原特钢装备制造有限公司 Smelting process of calendaring roller 20CrNiMo steel for manufacturing photovoltaic glass

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4898626A (en) 1988-03-25 1990-02-06 Armco Advanced Materials Corporation Ultra-rapid heat treatment of grain oriented electrical steel
JPH09104922A (en) 1995-10-05 1997-04-22 Nippon Steel Corp Production of grain-oriented silicon steel sheet extremely high in magnetic flux density
JPH09104923A (en) 1995-10-06 1997-04-22 Nippon Steel Corp Production of grain-oriented silicon steel sheet
JP3644130B2 (en) * 1996-05-24 2005-04-27 Jfeスチール株式会社 Method for producing grain-oriented electrical steel sheet
IT1284268B1 (en) * 1996-08-30 1998-05-14 Acciai Speciali Terni Spa PROCEDURE FOR THE PRODUCTION OF GRAIN ORIENTED MAGNETIC SHEETS, WITH HIGH MAGNETIC CHARACTERISTICS, STARTING FROM
IT1285153B1 (en) * 1996-09-05 1998-06-03 Acciai Speciali Terni Spa PROCEDURE FOR THE PRODUCTION OF GRAIN ORIENTED MAGNETIC SHEET, STARTING FROM THIN SHEET.
DE19745445C1 (en) * 1997-10-15 1999-07-08 Thyssenkrupp Stahl Ag Process for the production of grain-oriented electrical sheet with low magnetic loss and high polarization
JP4598702B2 (en) * 2006-03-23 2010-12-15 新日本製鐵株式会社 Manufacturing method of high Si content grain-oriented electrical steel sheet with excellent magnetic properties
WO2009091127A2 (en) * 2007-12-28 2009-07-23 Posco Grain oriented electrical steel having excellent magnetic properties and manufacturing method for the same
CN101768697B (en) * 2008-12-31 2012-09-19 宝山钢铁股份有限公司 Method for manufacturing oriented silicon steel with one-step cold rolling method
PL2418294T3 (en) * 2009-04-06 2020-06-01 Nippon Steel Corporation Method of treating steel for grain-oriented electrical steel sheet and method of manufacturing grain-oriented electrical steel sheet
JP4840518B2 (en) * 2010-02-24 2011-12-21 Jfeスチール株式会社 Method for producing grain-oriented electrical steel sheet
JP5772410B2 (en) * 2010-11-26 2015-09-02 Jfeスチール株式会社 Method for producing grain-oriented electrical steel sheet

Also Published As

Publication number Publication date
KR20150007360A (en) 2015-01-20
EP2876173B1 (en) 2018-10-24
EP2876173A4 (en) 2016-02-24
BR112013015997A2 (en) 2018-07-17
US20150170812A1 (en) 2015-06-18
WO2014013615A1 (en) 2014-01-23
CN103687966A (en) 2014-03-26
RU2593051C1 (en) 2016-07-27
EP2876173B8 (en) 2018-12-26
PL2876173T3 (en) 2019-04-30
BR112013015997B1 (en) 2019-06-25
JPWO2014013615A1 (en) 2016-06-30
EP2876173A1 (en) 2015-05-27
JP5423909B1 (en) 2014-02-19

Similar Documents

Publication Publication Date Title
EP2876173B9 (en) Manufacturing method of grain-oriented electrical steel sheet
JP6844125B2 (en) Manufacturing method of grain-oriented electrical steel sheet
EP2548977B1 (en) Method for producing directional electromagnetic steel sheet
EP2578706B1 (en) Method of manufacturing grain-oriented electrical steel sheet
EP2537946B1 (en) Method for manufacturing grain-oriented electrical steel sheet
KR101389248B1 (en) Manufacturing method for grain-oriented electromagnetic steel sheet
JP5757693B2 (en) Low iron loss unidirectional electrical steel sheet manufacturing method
KR101707451B1 (en) Grain oriented electrical steel sheet and method for manufacturing the same
KR101594601B1 (en) Oriented electrical steel sheets and method for manufacturing the same
KR20140084893A (en) Oriented electrical steel steet and method for the same
JP5862582B2 (en) Method for producing grain-oriented electrical steel sheet, grain-oriented electrical steel sheet and surface glass coating for grain-oriented electrical steel sheet
KR101568835B1 (en) Oriented electrical steel sheet and method for manufacturing the same
JP2011208196A (en) Method for manufacturing grain-oriented electromagnetic steel sheet having considerably low iron loss
JP7159594B2 (en) Manufacturing method of grain-oriented electrical steel sheet
JPH07138643A (en) Production of grain-oriented electrical steel sheet excellent in magnetic property
KR101459730B1 (en) Oriented electrical steel sheets and method for manufacturing the same

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20150220

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

DAX Request for extension of the european patent (deleted)
RA4 Supplementary search report drawn up and despatched (corrected)

Effective date: 20160126

RIC1 Information provided on ipc code assigned before grant

Ipc: C21D 8/12 20060101AFI20160120BHEP

Ipc: H01F 1/16 20060101ALI20160120BHEP

Ipc: C22C 38/06 20060101ALI20160120BHEP

Ipc: C22C 38/00 20060101ALI20160120BHEP

Ipc: C22C 38/60 20060101ALI20160120BHEP

17Q First examination report despatched

Effective date: 20161007

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: EXAMINATION IS IN PROGRESS

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: GRANT OF PATENT IS INTENDED

INTG Intention to grant announced

Effective date: 20180418

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

GRAT Correction requested after decision to grant or after decision to maintain patent in amended form

Free format text: ORIGINAL CODE: EPIDOSNCDEC

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602012052755

Country of ref document: DE

Ref country code: AT

Ref legal event code: REF

Ref document number: 1056729

Country of ref document: AT

Kind code of ref document: T

Effective date: 20181115

REG Reference to a national code

Ref country code: CH

Ref legal event code: PK

Free format text: BERICHTIGUNG B8

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20181024

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 1056729

Country of ref document: AT

Kind code of ref document: T

Effective date: 20181024

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

Ref country code: ES

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190124

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190224

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190124

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190125

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20190224

REG Reference to a national code

Ref country code: CH

Ref legal event code: PK

Free format text: BERICHTIGUNG B9

REG Reference to a national code

Ref country code: DE

Ref legal event code: R082

Ref document number: 602012052755

Country of ref document: DE

Representative=s name: VOSSIUS & PARTNER PATENTANWAELTE RECHTSANWAELT, DE

Ref country code: DE

Ref legal event code: R081

Ref document number: 602012052755

Country of ref document: DE

Owner name: NIPPON STEEL CORPORATION, JP

Free format text: FORMER OWNER: NIPPON STEEL & SUMITOMO METAL CORP., TOKYO, JP

REG Reference to a national code

Ref country code: DE

Ref legal event code: R026

Ref document number: 602012052755

Country of ref document: DE

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

PLAX Notice of opposition and request to file observation + time limit sent

Free format text: ORIGINAL CODE: EPIDOSNOBS2

26 Opposition filed

Opponent name: SMS GROUP GMBH

Effective date: 20190723

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

PLBB Reply of patent proprietor to notice(s) of opposition received

Free format text: ORIGINAL CODE: EPIDOSNOBS3

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

REG Reference to a national code

Ref country code: BE

Ref legal event code: MM

Effective date: 20190731

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190731

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190720

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190731

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190731

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20190720

REG Reference to a national code

Ref country code: DE

Ref legal event code: R100

Ref document number: 602012052755

Country of ref document: DE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

PLCK Communication despatched that opposition was rejected

Free format text: ORIGINAL CODE: EPIDOSNREJ1

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20120720

PLBN Opposition rejected

Free format text: ORIGINAL CODE: 0009273

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: OPPOSITION REJECTED

27O Opposition rejected

Effective date: 20210519

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20181024

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20240530

Year of fee payment: 13

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20240611

Year of fee payment: 13

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: PL

Payment date: 20240529

Year of fee payment: 13

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20240529

Year of fee payment: 13